NDC 51990-112

Galantamine Hydrobromide

Galantamine Hydrobromide

Galantamine Hydrobromide is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Yabao Pharmaceutical Co., Ltd. Beijing. The primary component is Galantamine Hydrobromide.

• Product ID: 51990-112_a602c1a5-0c9c-4489-bc71-5fd6e0b06cae
• NDC: 51990-112
• Product Type: Human Prescription Drug
• Proprietary Name: Galantamine Hydrobromide
• Generic Name: Galantamine Hydrobromide
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2001-03-01
• Marketing Category: NDA / NDA
• Application Number: NDA021169
• Labeler Name: Yabao Pharmaceutical Co., Ltd. Beijing
• Substance Name: GALANTAMINE HYDROBROMIDE
• Active Ingredient Strength: 8 mg/1
• Pharm Classes: Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 51990-112-02

100 TABLET, FILM COATED in 1 BOTTLE (51990-112-02)

• Marketing Start Date: 2001-03-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 51990-112-04 [51990011204]

Galantamine Hydrobromide TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA021169
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2001-03-01
• Inactivation Date: 2020-01-31

NDC 51990-112-03 [51990011203]

Galantamine Hydrobromide TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA021169
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2001-03-01
• Inactivation Date: 2020-01-31

NDC 51990-112-02 [51990011202]

Galantamine Hydrobromide TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA021169
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2001-03-01
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
GALANTAMINE HYDROBROMIDE	8 mg/1

OpenFDA Data

• SPL SET ID: 7dc963dd-84d6-45f3-857f-46a44fe9edc8
• Manufacturer:
  • Yabao Pharmaceutical Co., Ltd. Beijing
• UNII:
  • MJ4PTD2VVW
• RxNorm Concept Unique ID - RxCUI:
  • 579148
  • 310437
  • 310436
• UPC Code:
  • 0351990112045
  • 0351990111048
  • 0351990113042

Pharmacological Class

• Cholinesterase Inhibitor [EPC]
• Cholinesterase Inhibitors [MoA]

NDC Crossover Matching brand name "Galantamine Hydrobromide" or generic name "Galantamine Hydrobromide"

NDC	Brand Name	Generic Name
0054-0137	Galantamine Hydrobromide	Galantamine Hydrobromide
10147-0881	galantamine hydrobromide	galantamine hydrobromide
10147-0882	galantamine hydrobromide	galantamine hydrobromide
10147-0883	galantamine hydrobromide	galantamine hydrobromide
10147-0891	galantamine hydrobromide	galantamine hydrobromide
10147-0892	galantamine hydrobromide	galantamine hydrobromide
10147-0893	galantamine hydrobromide	galantamine hydrobromide
43353-984	Galantamine hydrobromide	Galantamine hydrobromide
47335-835	Galantamine Hydrobromide	Galantamine Hydrobromide
47335-836	Galantamine Hydrobromide	Galantamine Hydrobromide
47335-837	Galantamine Hydrobromide	Galantamine Hydrobromide
51990-112	Galantamine Hydrobromide	Galantamine Hydrobromide
51990-111	Galantamine Hydrobromide	Galantamine Hydrobromide
51990-113	Galantamine Hydrobromide	Galantamine Hydrobromide
21695-184	RAZADYNE	galantamine hydrobromide
21695-591	RAZADYNE	galantamine hydrobromide